rs143452727
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
C
Chromosome
11
Location
65720139
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_032193.4(RNASEH2C):c.374A>G (p.Asn125Ser)
Allele
C
Clinical Significance
Uncertain significance